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Red blood cell distribution width at admission predicts outcome in critically ill patients with kidney failure: a retrospective cohort study based on the MIMIC-IV database
PURPOSE: We aimed to explore whether red blood cell distribution width (RDW) could serve as a biomarker to predict outcomes in critically ill patients with kidney failure in this study. MATERIALS AND METHODS: This retrospective study was conducted with the Medical Information Mart for Intensive Care...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291648/ https://www.ncbi.nlm.nih.gov/pubmed/35834358 http://dx.doi.org/10.1080/0886022X.2022.2098766 |
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author | Hua, Rongqian Liu, Xuefang Yuan, Enwu |
author_facet | Hua, Rongqian Liu, Xuefang Yuan, Enwu |
author_sort | Hua, Rongqian |
collection | PubMed |
description | PURPOSE: We aimed to explore whether red blood cell distribution width (RDW) could serve as a biomarker to predict outcomes in critically ill patients with kidney failure in this study. MATERIALS AND METHODS: This retrospective study was conducted with the Medical Information Mart for Intensive Care IV (MIMIC-IV).A total of 674 patients were divided into three groups based on tertiles of RDW. We used the generalized additive model, Kaplan–Meier curve, and Cox proportional hazards models to evaluate the association between RDW and clinical outcomes. We then performed subgroup analyses to investigate the stability of the associations between RDW and all-cause mortality. RESULTS: Nonlinear and J-shaped curves were observed in the generalized additive model. Kaplan–Meier analysis showed that patients with elevated RDW had a lower survival rate. The Cox regression model indicated that high levels of RDW were most closely associated with ICU mortality and 30-day mortality (HR = 4.71, 95% CI: 1.69–11.64 and HR = 6.62, 95% CI: 2.84–15.41). Subgroup analyses indicated that the associations between RDW and all-cause mortality were stable. CONCLUSIONS: Elevated levels of RDW were associated with an increased risk of all-cause mortality, and RDW could be an independent prognostic factor for kidney failure. |
format | Online Article Text |
id | pubmed-9291648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-92916482022-07-19 Red blood cell distribution width at admission predicts outcome in critically ill patients with kidney failure: a retrospective cohort study based on the MIMIC-IV database Hua, Rongqian Liu, Xuefang Yuan, Enwu Ren Fail Clinical Study PURPOSE: We aimed to explore whether red blood cell distribution width (RDW) could serve as a biomarker to predict outcomes in critically ill patients with kidney failure in this study. MATERIALS AND METHODS: This retrospective study was conducted with the Medical Information Mart for Intensive Care IV (MIMIC-IV).A total of 674 patients were divided into three groups based on tertiles of RDW. We used the generalized additive model, Kaplan–Meier curve, and Cox proportional hazards models to evaluate the association between RDW and clinical outcomes. We then performed subgroup analyses to investigate the stability of the associations between RDW and all-cause mortality. RESULTS: Nonlinear and J-shaped curves were observed in the generalized additive model. Kaplan–Meier analysis showed that patients with elevated RDW had a lower survival rate. The Cox regression model indicated that high levels of RDW were most closely associated with ICU mortality and 30-day mortality (HR = 4.71, 95% CI: 1.69–11.64 and HR = 6.62, 95% CI: 2.84–15.41). Subgroup analyses indicated that the associations between RDW and all-cause mortality were stable. CONCLUSIONS: Elevated levels of RDW were associated with an increased risk of all-cause mortality, and RDW could be an independent prognostic factor for kidney failure. Taylor & Francis 2022-07-14 /pmc/articles/PMC9291648/ /pubmed/35834358 http://dx.doi.org/10.1080/0886022X.2022.2098766 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Hua, Rongqian Liu, Xuefang Yuan, Enwu Red blood cell distribution width at admission predicts outcome in critically ill patients with kidney failure: a retrospective cohort study based on the MIMIC-IV database |
title | Red blood cell distribution width at admission predicts outcome in critically ill patients with kidney failure: a retrospective cohort study based on the MIMIC-IV database |
title_full | Red blood cell distribution width at admission predicts outcome in critically ill patients with kidney failure: a retrospective cohort study based on the MIMIC-IV database |
title_fullStr | Red blood cell distribution width at admission predicts outcome in critically ill patients with kidney failure: a retrospective cohort study based on the MIMIC-IV database |
title_full_unstemmed | Red blood cell distribution width at admission predicts outcome in critically ill patients with kidney failure: a retrospective cohort study based on the MIMIC-IV database |
title_short | Red blood cell distribution width at admission predicts outcome in critically ill patients with kidney failure: a retrospective cohort study based on the MIMIC-IV database |
title_sort | red blood cell distribution width at admission predicts outcome in critically ill patients with kidney failure: a retrospective cohort study based on the mimic-iv database |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291648/ https://www.ncbi.nlm.nih.gov/pubmed/35834358 http://dx.doi.org/10.1080/0886022X.2022.2098766 |
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